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Background  

Nicotinic acetylcholine receptors (nAChRs) are pentameric proteins that are important drug targets for a variety of diseases including Alzheimer's, schizophrenia and various forms of epilepsy. One of the most intensively studied nAChR subunits in recent years has been α7. This subunit can form functional homomeric pentamers (α7)5, which can make interpretation of physiological and structural data much simpler. The growing amount of structural, pharmacological and physiological data for these receptors indicates the need for a dedicated and accurate database to provide a means to access this information in a coherent manner.  相似文献   
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Pulsed plasma polymerization of N-isopropylacrylamide leads to the deposition of thermoresponsive films. The reversible (switching) behavior of these poly(N-isopropylacrylamide) surfaces has been exemplified by screening the adsorption of fibrinogen and fluorescein isothiocyanate labeled bovine serum albumin proteins by surface plasmon resonance (SPR) and fluorescence microscopy at low and elevated temperatures.  相似文献   
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The results of a comprehensive investigation of the photophysical properties of the sunscreen analogue, N-acetyl menthyl anthranilate (NAMA), in various solvent systems are reported. Luminescence studies reveal that this compound is fluorescent (Phi(f)=0.16+/-0.01) in toluene and has a solvent dependent emission maximum in the range 363-370 nm. Phosphorescence has also been detected in low temperature glasses with an emission maximum at 420 nm in EPA, and a lifetime of 1.3 s; the triplet energy was found to be 311+/-3 kJ mol(-1). Kinetic UV-visible absorption measurements revealed a transient species with absorption maxima at 450 nm and solvent dependent lifetimes of 120-240 micros which are attributed to the triplet state. The triplet state is efficiently quenched by oxygen, leading to the formation of singlet oxygen in all of the solvent systems studied. The singlet oxygen quantum yields (Phi(Delta)), determined by time-resolved near-infrared luminescence measurements, were in the range 0.19-0.21.  相似文献   
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Studies are reported on a series of triphenylamine–(C?C)n–2,5‐diphenyl‐1,3,4‐oxadiazole dyad molecules (n=1–4, 1 , 2 , 3 and 4 , respectively) and the related triphenylamine‐C6H4–(C?C)3–oxadiazole dyad 5 . The oligoyne‐linked D–π–A (D=electron donor, A=electron acceptor) dyad systems have been synthesised by palladium‐catalysed cross‐coupling of terminal alkynyl and butadiynyl synthons with the corresponding bromoalkynyl moieties. Cyclic voltammetric studies reveal a reduction in the HOMO–LUMO gap in the series of compounds 1 – 4 as the oligoyne chain length increases, which is consistent with extended conjugation through the elongated bridges. Photophysical studies provide new insights into conjugative effects in oligoyne molecular wires. In non‐polar solvents the emission from these dyad systems has two different origins: a locally excited (LE) state, which is responsible for a π*→π fluorescence, and an intramolecular charge transfer (ICT) state, which produces charge‐transfer emission. In polar solvents the LE state emission vanishes and only ICT emission is observed. This emission displays strong solvatochromism and analysis according to the Lippert–Mataga–Oshika formalism shows significant ICT for all the luminescent compounds with high efficiency even for the longer more conjugated systems. The excited‐state properties of the dyads in non‐polar solvents vary with the extent of conjugation. For more conjugated systems a fast non‐radiative route dominates the excited‐state decay and follows the Engelman–Jortner energy gap law. The data suggest that the non‐radiative decay is driven by the weak coupling limit.  相似文献   
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The fluid dynamics behavior of shallow fluidized and vibrofluidized beds operating with fresh leaves was investigated with the aim of exploring drying applications in a modified conveyor belt (MCB) system,which may be operated in a fixedor fluidized-bed mode.Leaves of the specimens Duranta repens,Schinus molle,Coleus barbatus,Buxus sempervirens,and Bougainvillea spectabilis were tested with a range of sphericities from 0.063 to 0.213,bulk densities from 0.038 to 0.251 g/cm 3,apparent densities from 0.52 to ...  相似文献   
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We demonstrate that absolute measurements of the photoluminescence quantum yield of solutions can be made using an integrating sphere and a conventional fluorimeter. With this method the need for measurements against a luminescence standard is overcome. The sphere is mounted inside a commercial fluorimeter, which gives flexibility in excitation and emission wavelength ranges. A number of compounds have been investigated and the results are compared to literature values and data obtained using a comparative method.  相似文献   
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